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靶向髓系恶性肿瘤中凋亡失调——治疗革命的曙光。

Targeting apoptosis dysregulation in myeloid malignancies - The promise of a therapeutic revolution.

机构信息

Department of Biomedicine and Prevention, PhD in Immunology, Molecular Medicine and Applied Biotechnology, University of Rome Tor Vergata, 00133 Rome, Italy; Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.

Department of Biomedicine and Prevention, PhD in Immunology, Molecular Medicine and Applied Biotechnology, University of Rome Tor Vergata, 00133 Rome, Italy.

出版信息

Blood Rev. 2023 Nov;62:101130. doi: 10.1016/j.blre.2023.101130. Epub 2023 Aug 29.

Abstract

In recent years, the therapeutic landscape of myeloid malignancies has been completely revolutionized by the introduction of several new drugs, targeting molecular alterations or pathways crucial for leukemia cells survival. Particularly, many agents targeting apoptosis have been investigated in both pre-clinical and clinical studies. For instance, venetoclax, a pro-apoptotic agent active on BCL-2 signaling, has been successfully used in the treatment of acute myeloid leukemia (AML). The impressive results achieved in this context have made the apoptotic pathway an attractive target also in other myeloid neoplasms, translating the experience of AML. Therefore, several drugs are now under investigation either as single or in combination strategies, due to their synergistic efficacy and capacity to overcome resistance. In this paper, we will review the mechanisms of apoptosis and the specific drugs currently used and under investigation for the treatment of myeloid neoplasia, identifying critical research necessities for the upcoming years.

摘要

近年来,由于几种新药物的引入,针对白血病细胞生存至关重要的分子改变或途径的治疗方法,彻底改变了髓系恶性肿瘤的治疗格局。特别是,许多针对细胞凋亡的药物已在临床前和临床研究中进行了研究。例如,venetoclax 是一种针对 BCL-2 信号的促凋亡药物,已成功用于治疗急性髓系白血病 (AML)。在这方面取得的令人印象深刻的结果使得凋亡途径成为其他髓系肿瘤的一个有吸引力的靶点,这也转化了 AML 的经验。因此,由于其协同疗效和克服耐药性的能力,目前有几种药物正在作为单一或联合策略进行研究。本文将综述凋亡的机制以及目前用于治疗髓系肿瘤的特定药物,并确定未来几年的关键研究需求。

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